Actively Recruiting
Electronic Archive of Internal Medicine for the Treatment of Severe Organ Failure and Liver Transplantation-MITIGO
Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2025-01-17
10000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are conducting an observational study to collect and analyze data from patients diagnosed with acute or chronic liver failure, including those considered for liver transplantation. The study aims to gather both past and ongoing medical information to better understand the epidemiology, complications, hospitalizations, and treatment patterns related to severe liver disease. This research will take place at a single center and is sponsored by IRCCS Azienda Ospedaliero-Universitaria di Bologna. The study involves collecting retrospective data from patients diagnosed between January 1, 2013, and the study start date, followed by prospective data collection of patients diagnosed during the subsequent 10 years. There are no interventional treatments or drugs being tested; rather, the study focuses on gathering detailed medical records and treatment histories to observe outcomes and changes over time. Participants will have their medical records reviewed to classify liver disease types, track complications, hospitalizations, liver transplant evaluations, and transplant procedures over a 10-year period. Researchers will also describe prescribed treatments and monitor survival rates. There is no active treatment or procedure required from participants, and data collection is observational, based on standard clinical care and follow-up.
CONDITIONS
Brief Title
Electronic Archive of Internal Medicine for the Treatment of Severe Organ Failure and Liver Transplantation-MITIGO
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of acute or chronic liver disease or liver transplantation
- Age 18 years or older
- Ability to provide informed consent
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 10 years
Participants who have been diagnosed with acute or chronic liver failure are observed through structured collection of their medical records.
Trial Site Locations
Total: 1 location
1
IRCCS - Azienda Ospedaliero-Universitaria di Bologna
Bologna, Bologna, Italy, 40138
Actively Recruiting
Research Team
G
Giovanni Vitale, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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